FDA UDI In Commercial Distribution 🇺🇸 United States

HD+12

DI: 08056732652422 · Model: HD+12 · CARDIOLINE SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HD+12
Primary DI
08056732652422
Version / Model
HD+12
Catalog Number
81018331
Company Name
CARDIOLINE SPA
Labeler DUNS
339465174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-26
Public Version
1
Public Version Date
2025-03-06
Public Version Status
New
Public Device Record Key
e13319b6-0f0b-47c7-bc9f-3e7da978f21a

Device Description

Digital portable acquisition device which can acquire the electrocardiographic signal of 12 standard leads. Connected with a receiver via Bluetooth or USB, sends the data to the host.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

GMDN Terms

Code Name
16231 Electrocardiograph, professional, multichannel

Identifiers

Type ID
Primary 08056732652422

Customer Contacts

Phone
+39046196821

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Storage Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
54 – 106 KiloPascal
Type
Storage Environment Atmospheric Pressure
Temperature Range
54 – 106 KiloPascal